Background of the Invention
[0001] The present invention relates to a chemical solubilizing agent for tin or tin alloy
used for electroconductive materials such as, for example, in the manufacture of printed
circuit boards, electronic and electric devices.
[0002] With electric and mechanical development, the components for use in various devices
are being complicated and diversified. For example, in some printed circuit board
manufacturing process, tin or tin alloy is plated onto a copper foil layer, etching
is applied to unnecessary copper portions, then in a later stage the plated portion
alone is removed, and the operation shifts to the next step to form a high precision
circuit. Further, there are lead frames and copper wires plated with tin or tin alloy
or to which tin or tin alloy is bonded mechanically, and it is sometimes required
to remove such coating to expose the copper base as in the case of a printed circuit
board. For recovering useful metals such as copper from coating scraps in such manufacturing
process or from parts which have become unnecessary, the tin or tin alloy is first
removed and then copper is recovered through a copper refining process.
[0003] As a method for removing tin or tin alloy from the copper surface containing a copper
alloy there has been proposed a method which employs a solubilizing agent (i.e. solvent)
containing an oxidizing agent and an inorganic or organic acid as main components.
As an improvement over such method there is proposed in Japanese Patent Publication
Nos.40291/1977 and 40292/1977 a method which employs hydrogen peroxide or inorganic
peracid ion and acid and fluoride or iron ion as a chemical solubilizing agent for
tin-containing metals. Further, as a tin or tin alloy releasing solution there is
proposed in Japanese Patent Laid-Open No. 164984/1982 the use of an inorganic or
organic acid, an oxidizing agent and a heterocyclic compound of =NH or ≡N not containing
a sulfur atom. Further proposed are the combination of iron ion, a hydroxycarboxylic
acid and the above heterocyclic compound in Japanese Patent Laid-Open No. 58280/1983;
the combination of a fluorine-containing complex ion and the above heterocyclic compound
in Japanese Patent Laid-Open No. 74281/1984: the use of polyhydric alcohols in Japanese
Patent Laid-Open No.149790/1985; the combination of a fluorine-containing complex
iron, silicate iron and the above heterocyclic compound in Japanese Patent Laid-Open
No. 20470/1985; and the use of inorganic and organic acids, peroxides, and organic
acids which form a complex with tin ion. In the case of such solubilizing agent using
an oxidizing agent for tin or tin alloy, even a simple combination of an oxidizing
agent and an inorganic or organic acid dissolves tin or tin alloy relatively easily
in the initial stage, but with the lapse of time, tin and other metal ions accumulate
in the solubilizing agent solution, making the oxidizing agent unstable, or metallic
salts, particularly metastannic acid resulting from the oxidation of tin, precipitates
in the solution, so that the solubilizing ability of the solution deteriorates gradually.
To prevent this, as in the prior art referred to above, there has been proposed the
use of fluoride ion, a fluorine-containing complex, and an organic acid which forms
a complex with tin ion. Further, in some electroconductive materials it is required
that only a tin or tin alloy coating on the surface of a copper plate or copper wire
be melted and the copper surface be made difficult to dissolve. To this end it has
been proposed to use heterocyclic compounds of=NH or ≡N, e.g. pyrazole, imidazole,
triazole derivatives. It has also been proposed to use polyhydric alcohols in order
to enhance the luster of the copper surface.
[0004] In those solubilizing solutions, however, the dissolution speed of tin or tin alloy
is low, that is, the working efficiency is poor; besides, there often remains tin
on the copper surface. Moreover, with deterioration of the solubilizing solution and
the resulting increase of the tin concentration in the bath, hydrogen peroxide becomes
unstable, resulting in that the effect of the solubilizing solution is deteriorated.
[0005] It is the object of the present invention to eliminate the above-mentioned drawbacks
of the prior art, particularly to provide a solubilizing agent capable of dissolving
and removing tin or tin alloy from a copper surface rapidly and capable of stabilizing
hydrogen peroxide contained therein, as well as a method therefor.
Summary of the Invention
[0006] The present invention resides in a solubilizing agent for chemically dissolving tin
or tin alloy from electroconductive materials having a copper surface to which the
tin or tin alloy is fixed or electrodeposited. The solubilizing agent comprises an
acidic solution containing hydrogen peroxide and an inorganic acid, and 0.5-50 g/l
of one or more nitrogen-containing compounds selected from the group consisting of
heterocyclic compounds containing nitrogen and not containing a double bond in the
heterocyclic ring, cyclopentylamines and cyclohexylamines.
Detailed Description of the Invention
[0007] The following are concrete examples of selected nitrogen-containing compounds and
endocyclic amines in the present invention.
[0008] Heterocyclic compounds: pyrrolidine, 2-pyrrolidone, hydantoin, piperidine, piperazine
Cyclopentylamines: cyclopentylamine, 1-methyl-cyclopentylamine
Cyclohexylamines: cyclohexylamine, 1-methyl-cyclohexylamine
[0009] Examples of heterocyclic compounds also include those wherein hydrogen bonded to
a carbon atom in the ring is substituted by an alkyl group, such as pipecoline which
is a derivative of piperidine and 5,5-dimethylhydantoin which is a derivative of hydantoin.
[0010] The heterocyclic compounds already proposed are imidazole, triazole and pyrazole,
which have heretofore been used widely as copper inhibitors. But as a common point,
these compounds have double bonds in their rings as is apparent from the respective
structural formulae. As shown in Comparative Examples 2 and 3, these compounds do
not accelerate the dissolution of tin or tin alloy although they are superior in suppressing
the dissolution of copper.
[0011] The present invention is based on the finding that heterocyclic compounds not containing
a double bond are effective in improving the solubility of tin or tin alloy and that
among the amine compounds generally known as rust preventive agents for copper, endocyclic
amines, particularly cyclopentylamines and cyclohexylamines, are effective uniquely.
[0012] In the case where a heterocyclic compound or endocyclic amine used in the invention
is merely incorporated in the combination of hydrogen peroxide and an acid, the solubilizing
solution will be able to exhibit the desired effect in the initial stage just after
the preparation of the bath in which the solubilizing solution is not stained yet,
but as tin or tin alloy dissolves and accumulates in the bath so the solution is stained,
the hydrogen peroxide decomposes remarkably with the result that the dissolution speed
of the tin or tin alloy decreases rapidly. To prevent this, it is desirable to use
a stabilizer for the acidic hydrogen peroxide. Examples of such stabilizer include
glycol ethers such as, for example, ethylene glycol monomethyl ether, ethylene glycol
monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether,
diethylene glycol monoethyl ether and diethylene glycol monobutyl ether; saturated
aliphatic alcohols such as, for example, ethanol, n-propyl alcohol, n-butyl alcohol,
glycol and glycerin; aliphatic ethers such as, for example, ethyl ether and n-propyl
ether; aliphatic carboxylic acids such as, for example, propionic acid, aminobutyric
acid, aminocaproic acid and aminopropionic acid; aliphatic amines and imines such
as, for example, n-propylamine, isopropylamine, n-butylamine and n-hexylamine; and
acid amide-like compounds such as, for example, propionamide. Even if these compounds
are used together with the heterocyclic compounds or endocyclic amines which are employable
in the present invention, the respective effects will not be deteriorated and it will
be possible to af ford a chemical solubilizing solution free of the various problems
referred to above and high in productivity.
[0013] In the solubilizing agent of the present invention, the concentration of hydrogen
peroxide used as a basic component is preferably in the range of 1 to 10 g/l, and
preferred examples of inorganic acids which may be used in the invention are sulfuric
acid, nitric acid, phosphoric acid, sulfamic acid and hydrogen halides such as hydrofluoric
acid. The concentration of the inorganic acid used in the invention is not specially
limited provided it is not less than 10 g/l. But if it is too low, neutralization
will take place due to dissolved metal, so that the deterioration of the solubilizing
solution is accelerated, while a too high concentration thereof is not only uneconomical
but also causes an increase of the ion concentration in the aqueous solution, thus
permitting easier precipitation of dissolved metal. When these points are taken into
account, it is desirable to set the concentration of the inorganic acid used in the
invention in the range of 50 to 300 g/l. Sulfuric acid is easy to use because it is
relatively inexpensive. Phosphoric acid usually chelates with metal ions and stabilizes
H₂O₂ so its use is desirable. Sulfamic acid and hydrofluoric acid are useful for suppressing
the precipitation of dissolved tin or tin alloy. Particularly, for dissolving solder
which is a tin alloy, it is effective to use hydrofluorate and fluorate ions.
[0014] The dissolution accelerator used in the invention exhibits its effect in an amount
not less than 0.5g/l, but a too small amount thereof will cause an unstable condition
when tin ions are accumulated, while a too large amount thereof is uneconomical. A
preferred range is 1 to 10 g/l. Further, the concentration of the stabilizer for hydrogen
peroxide referred to previously is suitably in the range of 1 to 50 g/l.
[0015] In this way there is obtained a solution of a hydrogen peroxide inorganic acid system
particularly suitable for dissolving and removing tin or tin alloy. But this solution
can melt not only tin or tin alloy but also copper as the base material rapidly and
therefore, as in the prior art, a copper inhibitor such as, for example, imidazole,
pyrazole or triazole may be used as necessary together with the above components of
the solution.
[0016] The present invention will be described below in terms of working examples thereof.Materials
and Evaluation in the working examples:
(1) Materials to be Treated
[0017]
(a) Size 0.5 mm x 59 mm wide x 50 mm long
(b) Material
(i) both-side copper-clad laminate (copper 35 µ)
(ii) copper plate
(c) Thickness of tin or tin alloy plating
(i) tin plating 1.5 µ
(ii) tin alloy 2.0 µ (tin : lead = 60:40)
(2) Evaluation
[0018]
(a) Dissolution speed (min)
(b) Release of tin or tin alloy (visual)
ⓞ good
○ remains slightly (1-3%)
Δ remains a small amount (4-10%)
X remains a large amount (above 10%)
(c) Surface of the copper base (visual)
ⓞ good
○ somewhat good
Δ bad
X disapprobative
Example I
[0019] A sample of a copper plate plated 1.5 µ with tin was immersed at 40°C in 500 ml of
a solubilizing agent comprising an aqueous solution of 5 g/l H₂O₂ and 150 g/l H₂SO₄
and each of accelerators of Table 1 added 3 g/l into the said aqueous solution.
The dissolution speed of tin was determined and the dissolved state of tin and the
surface condition of copper were observed.
Table 1
|
Dissolution Accelerator |
Sn Disslution (min) |
Sn Release |
Cu Surface |
Comp. Ex. 1 |
- |
4′ 10˝ |
○ |
Δ |
Comp. Ex. 2 |
imidazole |
3′ 45˝ |
○ |
ⓞ |
Comp. Ex. 3 |
triazole |
4′ 05˝ |
○ |
ⓞ |
Comp. Ex. 4 |
glycolic acid |
5′ or more |
X |
X |
Comp. Ex. 5 |
aniline |
5′ or more |
X |
X |
Ex. 1 |
pyrrolidine |
2′ 07˝ |
ⓞ |
ⓞ |
Ex. 2 |
2-pyrrolidone |
1′ 58˝ |
○ |
○ |
Ex. 3 |
hydantoin |
1′ 48˝ |
○ |
Δ |
Ex. 4 |
5,5-dimethylhydantoin |
1′ 55˝ |
○ |
Δ |
Ex. 5 |
piperidine |
2′ 00˝ |
ⓞ |
ⓞ |
Ex. 6 |
piperazine |
1′ 59˝ |
|
|
Ex. 7 |
cyclopentylamine |
2′ 10˝ |
○ |
Δ |
Ex. 8 |
cyclohexylamine |
1′ 49˝ |
ⓞ |
○ |
Ex. 9 |
pipecoline |
2′ 15˝ |
ⓞ |
ⓞ |
Example II
[0020] A sample of an epoxy-based copper-clad laminate 35 µ in copper thickness plated 2.0
µ with the tin alloy was immersed at 40°C in 500 ml of solubilizing agent comprising
an aqueous solution containing 3 g/l H₂O₂, 100 g/l ammonium fluoride, 200 g/l borofluoric
acid and 5 g/l of each of the accelera-tors of Table 2 were added to the said aqueous
solution. The dissolution speed of the tin alloy was determined and the melting state
of the tin alloy and the surface condition of copper were observed.

Example III
[0021] In the step of removing tin from a sample of a copper plate plated 1.5 µ with tin,
using a solution consisting of 10 g/l H₂O₂ and 150 g/l H₂SO₄, when tin has dissolved
up to 30 g/l, the stability of hydrogen peroxide deteriorates even by an additional
supply of H₂O₂. To prevent this, the stabilizers shown in Table 3 were added and there
was made a comparison. In those (Comparative Examples 9-11) not containing the stabilizers,
there occurred a lowering of concentration due to the decomposition of H₂O₂ and the
melting speed of tin decreased. On the other hand, in those containing the stabilizers,
the dissolution speed was high and there was recognized no action impeding the effect
of the accelerators.
Table 3
|
Dissolution Acclerator |
Stablizer |
H2O2 Stability 40°C x 72 hr |
Sn Dissolution |
Sn Release |
Comp. Ex. 9 |
Pyrrolidine 2 |
not used |
43 % |
3′ 11˝ |
○ |
Comp. Ex. 10 |
piperidine 2 |
not used |
51 % |
3′ 05˝ |
○ |
Comp. Ex. 11 |
cyclohexylamine 2 |
not used |
48 % |
3′ 01˝ |
○ |
Ex.17 |
pyrrolidine 2 |
n-butyl alcohol |
87 % |
2′ 21˝ |
ⓞ |
Ex.18 |
piperidine 2 |
ethylene glycol monobutyl ether |
91 % |
2′ 16˝ |
ⓞ |
Ex.19 |
cyclohexylamine 2 |
propionamide |
85 % |
2′ 08˝ |
ⓞ |
Ex.20 |
cyclohexylamine 2 |
isopropylamine |
91 % |
2′ 15˝ |
ⓞ |
1. A chemical solubilizing agent for tin or a tin alloy, comprising an acidic solution
containing hydrogen peroxide and an inorganic acid and 0.5-50 g per liter of said
acidic solution of at least one nitrogen-containing compound selected from the group
consisting of heterocyclic compounds not having a double bond in a heterocyclic ring,
cyclopentylamines and cyclohexylamines.
2. A chemical solubilizing agent as set forth in Claim 1, wherein said nitrogen-containing
compound is pyrrolidine, 2-pyrrolidone, hydantoin, piperidine, piperazine, cyclopentylamine,
1-methylcyclopentylamine, cyclohexylamine, 1-methylcyclohexylamine, or a lower alkyl
substituted derivative thereof.
3. A chemical solubilizing agent as set forth in Claim 1, wherein the concentration
of the hydrogen peroxide in said acidic solution is in the range of 1 to 10 g/l.
4. A chemical solubilizing as set forth in Claim 1, wherein said inorganic acid is
sulfuric acid, nitric acid, phosphoric acid, sulfamic acid, or hydrogen halide.
5. A chemical solubilizing as set forth in Claim 1, wherein the concentration of the
inorganic acid in said acidic solution is not lower than 10 g/l.
6. A chemical solubilizing agent as set forth in Claim 1, further containing at least
one hydrogen peroxide stabilizing agent selected from the group consisting of alcohols,
glycol ethers, ethers, aliphatic amines and acid amides.
7. A process for treating and removing tin or a tin alloy adhered to a copper surface
containing a copper alloy, using a chemical solubilizing agent as claimed in any one
of Claims 1 to 6.